Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dzmtnvmt
    Member
    • Apr 2010
    • 11

    #1

    how to fetch the snp allele frequency?

    hello,everyone~

    I now need a txt file with several columns, which contains the rs ID of snp, frequency of each allele. I was told to download the SNPAlleleFreq.bcp file from ncbi. But i don't know exactly what each column tells about, and who to fetch the snp allel freq. So i need some help.

    thanks very much
  • epigen
    Senior Member
    • May 2010
    • 101

    #2
    Hi,

    if you haven't found another way yet, I'd recommend downloading the snp130 table from the UCSC genome browser. I suppose you'd like to have SNPs for the latest human genome? Then go to http://hgdownload.cse.ucsc.edu/golde...hg19/database/
    and download snp130.txt.gz

    A description of the columns is available in the "Tables"

    when you select from the dropdown menu
    group: Variations and Repeats track: SNPs (130)
    table: "snp130"
    and then hit "describe table schema"

    Hope this helps

    Comment

    • husamia
      Member
      • Apr 2010
      • 66

      #3
      I have the same question, I am interested in frequency information from dbsnp132. I have chromosomal positions and rs#s and want to get frequency information. My goal is to filter out common snps since 1000genomes data is supposed to discover rare variations <1%.

      Comment

      • megnetz
        Junior Member
        • Jul 2010
        • 4

        #4
        Hello! I checked one biallelic SNP in this database (snp131) to determine allele freq. I found an average heterozygosity of 0.5. I guess this is because there is no data on allele frequency? Or is it actually 0.5? In that case allele frequency should also be 0.5 according to hardy-weinberg?

        Thanks for your help!

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 10:05 AM
        0 responses
        8 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-13-2026, 12:22 PM
        0 responses
        33 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-11-2026, 10:35 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        38 views
        0 reactions
        Last Post SEQadmin2  
        Working...